Synthesis and in vitro evaluation of 4-substituted furano[3,2-c] tetrahydroquinolines as potential anti-cancer agents.
Article
Chen, Can, Zingales, Sarah, Wang, Ting et al. (2016). Synthesis and in vitro evaluation of 4-substituted furano[3,2-c] tetrahydroquinolines as potential anti-cancer agents.
. Journal of Enzyme Inhibition and Medicinal Chemistry, 31(5), 853-858. 10.3109/14756366.2015.1064120
Chen, Can, Zingales, Sarah, Wang, Ting et al. (2016). Synthesis and in vitro evaluation of 4-substituted furano[3,2-c] tetrahydroquinolines as potential anti-cancer agents.
. Journal of Enzyme Inhibition and Medicinal Chemistry, 31(5), 853-858. 10.3109/14756366.2015.1064120
A convenient and mild method for the synthesis of substituted furano [3,2-c]tetrahydroquinoline derivatives was developed, using the multi-component Povarov reaction. Of the synthesized tetrahydroquinoline derivatives, compound 10a displayed the greatest cellular proliferation inhibitory activities with IC50 values of 2.5-16.7 μmol/l. In addition, 10a induced murine C6 glioma cell apoptosis in a dose-dependent manner by up-regulating the expression of Bax, caspase-3, and caspase-9, and by down-regulating Bcl-2. Our findings suggest that these novel compounds have potential as therapeutic agents via inducing mitochondrial apoptosis.
